Method Validation Manager

2 weeks ago


Slough, United Kingdom Lonza Full time

Method Validation Manager Location: Slough, Hybrid Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of. The role We are looking for a Method Validation Manager to lead a team of up to 10 scientists and subject matter experts, in delivering customer method validation projects. You will ensure delivery is on time, on budget, and compliant with Lonza Biologics Safety and cGMP policies and regulations, supporting the Quality Control function. https://www.youtube.com/watch?v=wZaXzPKWEv0&list=PLh3u2rKfWyIfXC2d2O3enUrpMjjJ7DO_x&index=18 What you will get An agile career and dynamic working culture An inclusive and ethical workplace Compensation programs that recognize high performance A variety of benefits depending on role and location The full list of our global benefits can be found on https://www.lonza.com/careers/benefits What you will do Lead, coach, and mentor your team to support performance, recruitment, and retention Develop succession plans for yourself and your team Maintain training and skills to perform your duties effectively Create and manage work plans, resources, and schedules Troubleshoot technical issues and solve complex problems Monitor team overheads, BUP levels, and timesheet accuracy Identify and address training needs through Individual Development Plans (IDPs) Drive process improvement initiatives Deputise for the Head of Department and Head of QC Participate in quality and customer audits Ensure regulatory and safety compliance in the lab What we are looking for BSc in Biotechnology, Chemistry, or Chemical Engineering Extensive experience in Method validation Previous Biotech, CDMO or Pharmaceutical experience is essential for this role. Experience managing or supervising teams in Biologics/Pharma is highly desirable Physical chemistry and/or Bioassay proficiency is desirable Strong background in Quality Assurance or Quality Control within GMP-regulated environments is highly desirable Proven experience managing audits and inspections Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically. People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference. Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law. #J-18808-Ljbffr



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